Package 37808-775-02
Brand: cold head congestion severe
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
37808-775-02
Digits Only
3780877502
Product NDC
37808-775
Description
2 BLISTER PACK in 1 CARTON (37808-775-02) / 12 TABLET, COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
cold head congestion severe
Generic
acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2501bd52-2de5-3c3f-e063-6394a90acf49", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041220385874"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["c3849b66-697f-4f6e-93ab-76de031b3c70"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (37808-775-02) / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "37808-775-02", "marketing_start_date": "20180401"}], "brand_name": "Cold Head Congestion Severe", "product_id": "37808-775_2501bd52-2de5-3c3f-e063-6394a90acf49", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "37808-775", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Head Congestion Severe", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180401", "listing_expiration_date": "20261231"}